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在基于昆虫的无细胞系统中生产G蛋白偶联受体。

Production of G protein-coupled receptors in an insect-based cell-free system.

作者信息

Sonnabend Andrei, Spahn Viola, Stech Marlitt, Zemella Anne, Stein Christoph, Kubick Stefan

机构信息

Fraunhofer Institute for Cell Therapy and Immunology (IZI), Branch Bioanalysis and Bioprocesses Potsdam-Golm (IZI-BB), Am Muehlenberg 13, Potsdam 14476, Germany.

Department of Anesthesiology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

出版信息

Biotechnol Bioeng. 2017 Oct;114(10):2328-2338. doi: 10.1002/bit.26346. Epub 2017 Jul 3.

DOI:10.1002/bit.26346
PMID:28574582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5599999/
Abstract

The biochemical analysis of human cell membrane proteins remains a challenging task due to the difficulties in producing sufficient quantities of functional protein. G protein-coupled receptors (GPCRs) represent a main class of membrane proteins and drug targets, which are responsible for a huge number of signaling processes regulating various physiological functions in living cells. To circumvent the current bottlenecks in GPCR studies, we propose the synthesis of GPCRs in eukaryotic cell-free systems based on extracts generated from insect (Sf21) cells. Insect cell lysates harbor the fully active translational and translocational machinery allowing posttranslational modifications, such as glycosylation and phosphorylation of de novo synthesized proteins. Here, we demonstrate the production of several GPCRs in a eukaryotic cell-free system, performed within a short time and in a cost-effective manner. We were able to synthesize a variety of GPCRs ranging from 40 to 133 kDa in an insect-based cell-free system. Moreover, we have chosen the μ opioid receptor (MOR) as a model protein to analyze the ligand binding affinities of cell-free synthesized MOR in comparison to MOR expressed in a human cell line by "one-point" radioligand binding experiments. Biotechnol. Bioeng. 2017;114: 2328-2338. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc.

摘要

由于难以生产足够数量的功能性蛋白质,对人类细胞膜蛋白进行生化分析仍然是一项具有挑战性的任务。G蛋白偶联受体(GPCRs)是一类主要的膜蛋白和药物靶点,负责大量调节活细胞各种生理功能的信号传导过程。为了克服目前GPCR研究中的瓶颈,我们提出基于昆虫(Sf21)细胞提取物在真核无细胞系统中合成GPCR。昆虫细胞裂解物含有完全活跃的翻译和转运机制,允许对新合成的蛋白质进行翻译后修饰,如糖基化和磷酸化。在这里,我们展示了在真核无细胞系统中在短时间内以经济高效的方式生产几种GPCR。我们能够在基于昆虫的无细胞系统中合成分子量范围从40到133 kDa的多种GPCR。此外,我们选择了μ阿片受体(MOR)作为模型蛋白,通过“单点”放射性配体结合实验分析无细胞合成的MOR与在人细胞系中表达的MOR相比的配体结合亲和力。《生物技术与生物工程》2017年;114:2328 - 2338。©2017作者。《生物技术与生物工程》由威利期刊公司出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/31b3ff0cd8e5/BIT-114-2328-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/e57d32d0607b/BIT-114-2328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/683d32b5fe4a/BIT-114-2328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/546af131cdae/BIT-114-2328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/a16d58403f91/BIT-114-2328-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/31b3ff0cd8e5/BIT-114-2328-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/e57d32d0607b/BIT-114-2328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/683d32b5fe4a/BIT-114-2328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/546af131cdae/BIT-114-2328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/a16d58403f91/BIT-114-2328-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d639/5599999/31b3ff0cd8e5/BIT-114-2328-g006.jpg

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